Stephan Züchner

5.3k total citations
68 papers, 2.0k citations indexed

About

Stephan Züchner is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Stephan Züchner has authored 68 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Cellular and Molecular Neuroscience, 37 papers in Molecular Biology and 16 papers in Neurology. Recurrent topics in Stephan Züchner's work include Hereditary Neurological Disorders (25 papers), Genetic Neurodegenerative Diseases (21 papers) and Neurological diseases and metabolism (16 papers). Stephan Züchner is often cited by papers focused on Hereditary Neurological Disorders (25 papers), Genetic Neurodegenerative Diseases (21 papers) and Neurological diseases and metabolism (16 papers). Stephan Züchner collaborates with scholars based in United States, United Kingdom and Germany. Stephan Züchner's co-authors include Juan I. Young, Gaofeng Wang, Jeffery M. Vance, Alleene V. Strickland, Vincent Timmerman, Adriana Rebelo, Rebecca Schüle, Eden R. Martin, Warren D. Taylor and Kousik Krishnan and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Stephan Züchner

66 papers receiving 1.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stephan Züchner United States 23 854 853 397 381 284 68 2.0k
Ali Benomar Morocco 21 1.5k 1.7× 1.7k 2.0× 346 0.9× 709 1.9× 178 0.6× 69 2.3k
Mériem Tazir Algeria 21 1.0k 1.2× 948 1.1× 437 1.1× 473 1.2× 415 1.5× 47 2.1k
Roman Chrast Switzerland 35 1.8k 2.1× 1.1k 1.3× 426 1.1× 356 0.9× 538 1.9× 70 3.3k
Viviana Caputo Italy 23 863 1.0× 439 0.5× 208 0.5× 643 1.7× 145 0.5× 52 1.8k
Flavia Trettel Italy 28 1.4k 1.6× 1.2k 1.4× 604 1.5× 276 0.7× 112 0.4× 44 2.5k
Serena Giannelli Italy 24 1.3k 1.5× 516 0.6× 290 0.7× 216 0.6× 102 0.4× 33 1.9k
Tu‐Hsueh Yeh Taiwan 29 1.2k 1.4× 875 1.0× 373 0.9× 903 2.4× 168 0.6× 74 2.3k
Daniel J. Liebl United States 26 886 1.0× 1.3k 1.6× 228 0.6× 227 0.6× 199 0.7× 60 2.4k
Steven T. Suhr United States 20 1.6k 1.9× 1.1k 1.3× 191 0.5× 122 0.3× 121 0.4× 27 2.7k
Simon Stott United Kingdom 22 982 1.1× 605 0.7× 273 0.7× 458 1.2× 113 0.4× 34 1.9k

Countries citing papers authored by Stephan Züchner

Since Specialization
Citations

This map shows the geographic impact of Stephan Züchner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stephan Züchner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephan Züchner more than expected).

Fields of papers citing papers by Stephan Züchner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephan Züchner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stephan Züchner. The network helps show where Stephan Züchner may publish in the future.

Co-authorship network of co-authors of Stephan Züchner

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Züchner. A scholar is included among the top collaborators of Stephan Züchner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephan Züchner. Stephan Züchner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Koutsis, Georgios, David Pellerin, Pablo Iruzubieta, et al.. (2024). Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms. Journal of the Neurological Sciences. 467. 123309–123309. 2 indexed citations
3.
Pellerin, David, Marcus Vinícius Della Coletta, Mariana Spitz, et al.. (2024). Frequency of GAA-FGF14 ataxia in a large cohort of Brazilian patients with unsolved adult-onset cerebellar ataxia. Parkinsonism & Related Disorders. 122. 106157–106157. 3 indexed citations
4.
Li, Limin, Manoj P. Menezes, Melanie Smith, et al.. (2024). Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literature. Neuromuscular Disorders. 37. 29–35. 2 indexed citations
5.
Pellerin, David, Matt C. Danzi, Céline Bonnet, et al.. (2024). Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 52(5). 868–870. 1 indexed citations
6.
Pellerin, David, Pablo Iruzubieta, Marie‐Josée Dicaire, et al.. (2024). The FGF14 GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations. Clinical Genetics. 105(4). 446–452. 12 indexed citations
7.
Rebelo, Adriana, Lassana Cissé, Lynette Rives, et al.. (2023). Novel variant in CADM3 causes Charcot–Marie–Tooth disease. Brain Communications. 5(5). fcad227–fcad227. 2 indexed citations
8.
Reilly, Mary M., David N. Herrmann, Davide Pareyson, et al.. (2023). Trials for Slowly Progressive Neurogenetic Diseases Need Surrogate Endpoints. Annals of Neurology. 93(5). 906–910. 12 indexed citations
9.
Pellerin, David, Pedro José Tomaselli, Mariana Spitz, et al.. (2023). Frequency of GAA- FGF14 Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia. Neurology Genetics. 9(5). e200094–e200094. 17 indexed citations
10.
Wu, Tong, Davide Pareyson, Richard A. Lewis, et al.. (2023). Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history. Brain. 146(9). 3826–3835. 10 indexed citations
11.
Busseau, Isabelle, et al.. (2021). Translesion DNA synthesis-driven mutagenesis in very early embryogenesis of fast cleaving embryos. Nucleic Acids Research. 50(2). 885–898. 5 indexed citations
12.
Stregapede, Fabrizia, Lorena Travaglini, Adriana Rebelo, et al.. (2019). Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clinical Genetics. 97(3). 521–526. 11 indexed citations
13.
Manganelli, Fiore, Silvia Parisi, Maria Nolano, et al.. (2019). Insights into the pathogenesis of ATP1A1‐related CMT disease using patient‐specific iPSCs. Journal of the Peripheral Nervous System. 24(4). 330–339. 4 indexed citations
14.
Howell, R. Rodney & Stephan Züchner. (2018). MOVR—NeuroMuscular ObserVational Research, a unified data hub for neuromuscular diseases. Genetics in Medicine. 21(3). 536–538. 6 indexed citations
15.
Jacquier, Arnaud, Cécile Delorme, Edwige Belotti, et al.. (2017). Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death. Acta Neuropathologica Communications. 5(1). 55–55. 18 indexed citations
16.
Züchner, Stephan & Feifei Tao. (2015). DNM2-Related Intermediate Charcot-Marie-Tooth Neuropathy. 1 indexed citations
17.
Young, Juan I., Stephan Züchner, & Gaofeng Wang. (2015). Regulation of the Epigenome by Vitamin C. Annual Review of Nutrition. 35(1). 545–564. 241 indexed citations
18.
Sly, Laura M., Joshua Hersheson, Alejandro Horga, et al.. (2014). Extended phenotypic spectrum of KIF5A mutations. UCL Discovery (University College London). 3 indexed citations
19.
Taylor, Warren D., Stephan Züchner, Douglas R. McQuoid, et al.. (2007). Allelic Differences in the Brain-Derived Neurotrophic Factor Val66Met Polymorphism in Late-Life Depression. American Journal of Geriatric Psychiatry. 15(10). 850–857. 72 indexed citations
20.
Züchner, Stephan & Jeffery M. Vance. (2006). Mechanisms of Disease: a molecular genetic update on hereditary axonal neuropathies. Nature Clinical Practice Neurology. 2(1). 45–53. 77 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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